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RLM Consulting provides regulatory affairs support at all stages of the medicinal product development, from discovery research through preclinical and clinical testing, up to and beyond submission of the dossier required for marketing authorization. Our experienced staff provide strategic guidance to achieve the most appropriate regulatory scenario as well as practical feedback to drive the development of medicinal products. We have extensive experience in writing and negotiating with national agencies and the EMA and providing briefing documents for scientific advice requests, orphan drug designation dossiers, advanced therapy medicinal status, clinical trial applications (IMPD, IB) and marketing authorization applications with the...
Consulting,regulatory strategy,biotech products,submissions,interaction with regulatory bodies,and cell therapy
Rlm consulting operates in the Biotechnology research industry.
Rlm consulting's revenue is 11m - 100m
Rlm consulting has 11 - 50 employees.
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